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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Type Device Class Implantable

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No Description
BIOMET SPINE LLC
8601-4008
In Commercial Distribution

  • 00888480558408 ()

  • SPACER MPF PEEK 0° 40L X 18W X 8HMM
8601-4008

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-1518
In Commercial Distribution

  • 00888480558187 ()

  • ALIF PEEK 15° 30X40X18MM
8518-1518

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-0712
In Commercial Distribution

  • 00888480558057 ()

  • ALIF PEEK 7° 30X40X12MM
8518-0712

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-0020
In Commercial Distribution

  • 00888480558040 ()

  • ALIF PEEK 0° 30X40X20MM
8518-0020

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-0016
In Commercial Distribution

  • 00888480558026 ()

  • ALIF PEEK 0° 30X40X16MM
8518-0016

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8518-0012
In Commercial Distribution

  • 00888480558002 ()

  • ALIF PEEK 0° 30X40X12MM
8518-0012

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8512-0720
In Commercial Distribution

  • 00888480557296 ()

  • ALIF PEEK 7° 27X36X20MM
8512-0720

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8512-0714
In Commercial Distribution

  • 00888480557265 ()

  • ALIF PEEK 7° 27X36X14MM
8512-0714

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8618-6020
In Commercial Distribution

  • 03662663057301 ()

  • Spacer MPF PEEK 25° 60L x 22W x 20H
8618-6020

  • Polymeric spinal interbody fusion cage
No Description
BIOMET SPINE LLC
8618-6018
In Commercial Distribution

  • 03662663057295 ()

  • SPACER MPF PEEK 25° 60L X 22W
8618-6018

  • Polymeric spinal interbody fusion cage
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